Guidant Corporation
Guidant Corporation holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2006.
Top product codes for Guidant Corporation
Recent clearances by Guidant Corporation
- K060449 — HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIRE
- K053459 — OMNILINK .035 BILIARY STENT SYSTEM
- K053454 — RX HERCULINK ELITE BILIARY STENT SYSTEM
- K053019 — ACUITY STEERABLE STYLET ACCESSORY
- K052965 — EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832.
- K052274 — GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000
- K052166 — MODIFICATION TO: RX ACCUNET EMBOLIC PROTECTION SYSTEM
- K052165 — RX ACCUNET EMBOLIC PROTECTION SYSTEM
- K041981 — GUIDANT VASOVIEW 6 HARVESTING CANNULA, MODEL VH-2000; GUIDANT VASOVIEW 6 ACCESSORY PACK, MODEL VH-2004
- K041762 — FINISHING WIRE SUPPORTRAK
- K041574 — CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020
- K031903 — RAPIDO CUT-AWAY BLEEDBACK CONTROL VALVE (BBCV), MODEL 7568
- K032530 — MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM
- K031688 — RAPIDO CUT-A-WAY ROTATING HEMOSTASIS VALVE
- K031505 — RAPIDO CUT-AWAY GUIDING CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.